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Found 12 of ic50 for drug = Ambenyl
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  10nMAssay Description:50% Inhibition of stereospecific [3H]-naltrexone (10e-9 M) binding towards opiate receptor in rat brain homogenateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  105nMAssay Description:Tested for effective concentration against cloned human Opioid receptor mu 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetDelta-type opioid receptor(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50: >9.30E+3nMAssay Description:In vitro binding affinity against cloned human Opioid receptor delta 1 expressed in HEK 293S cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  1.00E+4nMAssay Description:Concentration required to inhibit [3H]naltrexone binding to Opioid receptorsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  1.50E+4nMAssay Description:In vitro binding affinity against cloned human Opioid receptor kappa 1 expressed in HEK 293S cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCytochrome P450 2D6(Homo sapiens (Human))
Vrije Universiteit

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  1.04E+5nMAssay Description:Inhibition of MAMC O-dealkylation mediated by human Cytochrome P450 2D6 expressed in human lymphoblastoid cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 1(Homo sapiens (Human))
University Medicine Greifswald

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  2.36E+5nMAssay Description:Inhibition of human OCT1 expressed in HEK293 cells assessed as reduction in ASP+ substrate uptake by microplate reader based analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D26(Rattus norvegicus)
Vrije Universiteit

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  2.38E+5nMAssay Description:Inhibition of MAMC O-dealkylation mediated by rat Cytochrome P450 2D2 expressed in Saccharomyces cerevisiaeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Reverse Proteomics Research Institute

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  3.02E+5nMAssay Description:Inhibitory concentration against potassium channel HERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D1(Rattus norvegicus)
Vrije Universiteit

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  1.32E+6nMAssay Description:Inhibition of MAMC O-dealkylation mediated by rat Cytochrome P450 2D1 expressed in Saccharomyces cerevisiaeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D4(Rattus norvegicus)
Vrije Universiteit

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  2.22E+6nMAssay Description:Inhibition of MAMC O-dealkylation mediated by rat Cytochrome P450 2D4 expressed in Saccharomyces cerevisiaeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D3(Rattus norvegicus)
Vrije Universiteit

Curated by ChEMBL
LigandPNGBDBM50019351((-)-Codeine | (Codeine) | (codeine)10-methoxy-4-me...)
Affinity DataIC50:  4.09E+6nMAssay Description:Inhibition of MAMC O-dealkylation mediated by rat Cytochrome P450 2D3 expressed in Saccharomyces cerevisiaeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed